SURBHI CHAUHAN

Ensured the timely submission of EC dossier and all other trial related documents to the Ethics Committee. Conducted a comprehensive review of CRFs, cross-referencing them with source documents. Monitored sites to maintain compliance with effective clinical research standards and GCP requirements. Performed Site selection, Site Initiation, Site Monitoring, and Site Close Out Visits as part of comprehensive clinical research site assessment.

Secured 90% data accuracy prior to reporting to sponsor and other core team members.. Monitored research sites to ensure 100% adherence to effective clinical research standards and Good Clinical Practice (GCP) requirements. Organized meetings with investigator group conferences, and special events to facilitate collaboration and knowledge sharing among research team members. Collaborated with the team to guarantee a seamless transition from study initiation to implementation.

Implemented quality control measures for research methodologies, resulting in a reduction of errors and biases by 90%. Prepared comprehensive reports and presentations using Microsoft Word and PowerPoint. Conducted surveys; interviews and experimental research to facilitate data analysis and reduced the missingness of data by 95%.

Processed, and delivered specimens from trial participants and also Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants. Placed orders for medications to be used in the studies, ensuring their availability and adherence to study protocols. Monitored subject enrollment, maintaining a 95% enrollment rate, and effectively tracked dropout details.

Maintained various logs, forms, and the site master file in strict accordance with the research protocol and organized documentation of study-related activities and conducted SAE reporting to sponsor and Regulatory authorities. Performed dose calculations for chemotherapy of patients and guaranteeing precise and safe administration of medication. Efficiently managed the inventory of supplies utilized for trial procedures, leading to a 95% availability rate of required supplies.

Attended 4 monitoring visits and 2 End of Study visits and patient visits. Performed Informed Consent Process With Approx.45 subjects. Proficiently worked on electronic case report forms (eCRF) as well as paper-based case report forms (CRF) resulting in a 98% accuracy rate for data collection and entry.